CYTOKINE-INDUCIBLE EXPRESSION IN ENDOTHELIAL-CELLS OF AN I-KAPPA-B-ALPHA-LIKE GENE IS REGULATED BY NF-KAPPA-B

被引:309
作者
DEMARTIN, R [1 ]
VANHOVE, B [1 ]
CHENG, Q [1 ]
HOFER, E [1 ]
CSIZMADIA, V [1 ]
WINKLER, H [1 ]
BACH, FH [1 ]
机构
[1] HARVARD UNIV,SCH MED,SANDOZ CTR IMMUNOBIOL,BOSTON,MA 02115
关键词
ENDOTHELIAL CELLS; INFLAMMATION; I-ALEPH-B/NF-ALEPH-B;
D O I
10.1002/j.1460-2075.1993.tb05938.x
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The transient expression of many different genes is mediated by the inducible transcription factor p50-p65 NFchiB, which in turn is regulated by, complex formation with its inhibitor IchiBalpha. We describe here that in porcine aortic endothelial celts, either IL-1alpha, TNFalpha or LPS upregulates an inhibitor of NFchiB which we refer to as ECI-6. ECI-6 is by structural and functional criteria an IchiBalpha protein, the porcine homologue of MAD-3, pp40 and RL/IF-1. We have studied the promoter of the ECI-6/IchiBalpha gene and provide three lines of evidence that its expression is directly regulated by NFchiB. First, the 5' regulatory region of ECI-6/IchiBalpha contains two sites that bind NFchiB in electrophoretic mobility shift assays. Second, expression following transfection of an ECI-6/IchiBalpha promoter-luciferase reporter construct is dependent on a co-transfected NFchiB-p65 subunit. Third, pretreatment of endothelial cells with antioxidants, agents that inhibit activation of NFchiB, inhibit the expression of ECI-6/IchiBalpha. We conclude that the regulated expression of ECI-6/IchiBalpha could represent a novel feedback mechanism by which NFchiB downregulates its own activity after transient activation of target genes has been achieved.
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页码:2773 / 2779
页数:7
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